HCMV targets the metabolic stress response through activation of AMPK whose activity is important for viral replication

• Published in: PLoS pathogens 2012-01, Vol.8 (1), p.e1002502-e1002502
• Main Authors: McArdle, Jessica, Moorman, Nathaniel J, Munger, Joshua
• Format: Article
• Language: English
• Subjects: Adenylic acid; Biology; Calcium-Calmodulin-Dependent Protein Kinase Kinase - genetics; Calcium-Calmodulin-Dependent Protein Kinase Kinase - metabolism; Cell Line; Cytomegalovirus - physiology; Cytomegalovirus Infections - genetics; Cytomegalovirus Infections - metabolism; Cytomegaloviruses; DNA replication; DNA, Viral - biosynthesis; Enzyme Activation; Enzymes; Gene Expression Regulation, Viral - genetics; Genetic aspects; Glycolysis; Humans; Kinases; Medicine; Microbiology; Physiological aspects; Protein kinases; Protein Kinases - genetics; Protein Kinases - metabolism; Proteins; Stress, Physiological; Viral genetics; Virus Replication
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1002502

Human Cytomegalovirus (HCMV) infection induces several metabolic activities that have been found to be important for viral replication. The cellular AMP-activated protein kinase (AMPK) is a metabolic stress response kinase that regulates both energy-producing catabolic processes and energy-consuming anabolic processes. Here we explore the role AMPK plays in generating an environment conducive to HCMV replication. We find that HCMV infection induces AMPK activity, resulting in the phosphorylation and increased abundance of several targets downstream of activated AMPK. Pharmacological and RNA-based inhibition of AMPK blocked the glycolytic activation induced by HCMV-infection, but had little impact on the glycolytic pathway of uninfected cells. Furthermore, inhibition of AMPK severely attenuated HCMV replication suggesting that AMPK is an important cellular factor for HCMV replication. Inhibition of AMPK attenuated early and late gene expression as well as viral DNA synthesis, but had no detectable impact on immediate-early gene expression, suggesting that AMPK activity is important at the immediate early to early transition of viral gene expression. Lastly, we find that inhibition of the Ca²⁺-calmodulin-dependent kinase kinase (CaMKK), a kinase known to activate AMPK, blocks HCMV-mediated AMPK activation. The combined data suggest a model in which HCMV activates AMPK through CaMKK, and depends on their activation for high titer replication, likely through induction of a metabolic environment conducive to viral replication.